Method, system and device for treating disorders of the pelvic floor by electrical stimulation of and the delivery of drugs to the left and right pudendal nerves

ABSTRACT

Described are devices and methods for treating various disorders of the pelvic floor by means of electrical stimulation of the pudendal nerves, and means for delivering one or more drugs in association with such electrical stimulation therapies. One or more electrical stimulation signals are applied, and one or more drugs are infused, injected or otherwise administered, to appropriate portions of a patient&#39;s pelvic floor and the pudendal nerves or portions thereof in an amount and manner effective to treat a number of disorders, including, but not limited to, urinary voiding dysfunction, fecal voiding dysfunction, constipation, stress incontinence, urge incontinence, urinary retention disorder, sexual dysfunction, orgasmic dysfunction, erectile dysfunction, pelvic pain, prostatitis, prostatalgia and prostatodynia.

RELATED APPLICATIONS

This application is a continuation-in-part of each of the following U.S.Patent Applications, and claims priority and other benefits from eachsuch Application: (1) U.S. patent application Ser. No. 10/236,578 toGerber et al. entitled “Electrical and/or Magnetic Stimulation Therapyfor the Treatment of Prostatitis and Prostatodynia” filed Sep. 6, 2002(2) U.S. patent application Ser. No. 10/723,316 to Spinelli et al.entitled “Method, System and Device for Treating Disorders of the PelvicFloor by Means of Electrical Stimulation of the Pudendal Nerves andAssociated Nerves, and the Optional Delivery of Drugs in AssociationTherewith” filed Nov. 26, 2003, which claims the benefit of U.S.Provisional Application No. 60/459,077 also to Spinelli et al. andhaving the same title filed Mar. 31, 2003; (3) U.S. patent applicationSer. No. 10/723,903 to Gerber entitled “Method, System and Device forTreating Various Disorders of the Pelvic Floor by Electrical Stimulationof the Pudendal Nerves and the Sacral Nerves at Different Sites” filedNov. 26, 2003; and (4) U.S. patent application Ser. No. 10/745,757 toGerber entitled “Method, System and Device for Treating VariousDisorders of the Pelvic Floor by Electrical Stimulation of the Left andRight Pudendal Nerves” filed Dec. 23, 2003. This application herebyincorporates by reference herein the foregoing '578, '316, '903 and '757patent applications, and the '077 provisional application, each in itsrespective entirety.

FIELD OF THE INVENTION

This invention relates to methods, systems and devices for treatingvarious disorders of the pelvic floor by delivering electrical stimuliand/or drugs to the pudendal nerves or portions thereof.

BACKGROUND

The medical device industry produces a wide variety of electronic andmechanical devices for treating patient medical conditions. Dependingupon the medical condition, medical devices may be surgically implantedor connected externally to a patient receiving treatment. Clinicians usemedical devices alone or in combination with drug therapies and surgeryto treat patient medical conditions. For some medical conditions,medical devices provide the best (and sometimes the only) therapy torestore an individual to a more healthful condition and a fuller life.Conditions that medical devices may effectively treat include pelvicfloor disorders.

Pelvic floor disorders adversely affect the health and quality of lifeof millions of people. Pelvic floor disorders include urinary controldisorders such as urge incontinency, urge frequency, voiding efficiency,fecal control disorders, sexual dysfunction, and pelvic pain.Individuals with urinary control disorders often face debilitatingchallenges in their everyday lives. These individuals may be preoccupiedwith trips to the bathroom, fears of embarrassment and sleepless nights.Some suffers become so anxious that they become isolated and depressed.Pelvic floor disorders may be treated with a variety of therapeuticoptions such as behavior modification including biofeedback,pharmacological treatment, mechanical intervention such asself-catheterization, physical appliances such as diapers, and surgicalintervention. Surgical treatments are the most invasive and are oftenconsidered after other therapies have proven ineffective.

Urinary incontinence, or the inability to control the passage of urine,is a relatively common problem. Although there are a variety ofdifferent types of urinary incontinence, stress incontinence, urgeincontinence and urinary retention are the most common.

Stress incontinence is the unacceptable passage of urine under thestress of increased abdominal pressure. This increased pressuretypically results from coughing, sneezing, and Valsalva. Stressincontinence is manifested urologically by normal cystometry, obtuseurethral vesicular angle, abnormally low urethral pressures and aphysiologically short urethral length. This disorder is most common inmultiparous, post-menopausal females. Physiologically, stressincontinence is a disorder of the volitional muscular control of theurethral resistance to the flow of urine. Laxity and partial denervationof the pelvic musculature is the chief abnormality.

Urge incontinence is the involuntary passage of urine with a concomitantsense of urgency. Systometry indicates detrusor (bladder wall muscle)contractions with low bladder filling pressures and volumes. Thesebladder contractions may not be inhibited in the presence of voluntaryEMG signals from the sphincter, indicating reduction or loss of thepudendal-parasympathetic inhibitory reflex. Unsolicited, prematurebladder contraction may result from mucosal irritation of variedetiology. These premature contractions of the bladder may also be theresult of an abnormally high gain in the detrusor contractile reflex dueto the loss of inhibitory control with an upper-motor-neuron lesion.

Urinary retention is characterized by the inability of a patient tospontaneously and controllably urinate or void. Catheterization of theurethra is provided to many patients suffering from urinary retention,which is often a painful and somewhat lengthy procedure having the addedrisk of causing infection.

Constipation is a life-disturbing problem that afflicts millions ofAmericans, from the very young to the elderly. Although relatively rareamong the young, it is a very common problem in middle age, and is anearly ubiquitous problem in the elderly. Chronic constipation is amajor problem for many individuals, and frequently causes extremediscomfort to the afflicted. Such discomfort may be a major obstacle toleading a normal life, and may consume an enormous amount of theafflicted person's energy and time.

Besides causing severe discomfort, chronic constipation may also beharmful to the patient. For example, chronic constipation may result inan intestinal obstruction that may cause the patient great pain; or thatmay even cause the patient's death, unless surgically corrected. Chronicconstipation may also prevent the patient from receiving the benefit ofcertain needed prescription medications, because the medications mayhave undesirable side effects on an already constipated gut.

Conventional therapies for chronic constipation are often distastefuland unpleasant at best, since they may involve treatments such asrepeated consumption of large quantities of laxatives, repetitive use ofenemas, or both. Repeatedly consuming large quantities of laxatives maybe harmful to the patient, since they may result in dehydration or evenrenal failure. The repetitive use of enemas may be harmful since theymay irritate or physically harm the treated portion of the patient'sgut.

Chronic constipation is usually thought of in association with problemsof the large intestine. Other parts of the patient's gut, however, mayalso exhibit chronic constipation-like problems, such as the esophagus,the stomach, and less frequently, the small intestine. Problemsassociated with chronic constipation may include depressed motility ofthe esophagus, stomach or small intestine. For simplicity, chronicconstipation, or chronic constipation-like problems, of any portion ofthe patient's gut from the esophagus to the anus will be referred tohereafter as simply “constipation”.

The prostate is a glandular and fibromuscular organ in the male, whichlies immediately below the bladder and surrounds the urethra.Prostatitis, the third leading disease of the prostate, is a commonurologic condition that many clinicians find difficult to treateffectively.

The main symptom of chronic prostatitis (category III) is pain, followedby variable voiding (urgency/frequency) and erectile or sexualdysfunction. Patients have symptoms such as painful ejaculation or painin the penis, testicles, or scrotum; low back, rectal or perineal pain;pain along the inner aspects of the thighs; irritative or obstructiveurinary symptoms; and decreased libido or impotence. As a rule, chronicnon-bacterial prostatitis patients do not have recurrent urinary tractinfections.

Chronic prostatitis is a major male health issue. The average urologistin the U.S. sees 173 prostatitis patients per year, of which one-thirdare newly diagnosed. The prevalence of prostatitis in the general malepopulation is estimated to be 5-8.8%, and it has been estimated thatabout 2 million office visits per year are related to prostatitis.Self-reported histories of prostatitis are as prevalent as 16% of allreported cases. Patients with chronic prostatitis experience a negativeimpact on quality of life comparable to patients with unstable angina,recent myocardial infarction or active Crohn's disease. The average ageof the prostatitis population is estimated at 50 years. Prostatitis isthe most common urologic diagnosis in men under 50 years old and thethird most common in men over 50 years old. The most commonclassification of prostatitis is chronic prostatitis/chronic pelvic painsyndrome (category III), which may include as many as 90% of allpatients who meet the criteria of the condition.

Despite the widespread prevalence of prostatitis, the diagnosis ofchronic prostatitis represents a particular challenge since itsdiagnosis is often based on exclusion. Prostatitis remains poorlyunderstood despite its prevalence because it encompasses multiplediverse disorders that cause symptoms related to the prostate gland. Theetiology of acute and chronic bacterial prostatitis is clearly defined,and is a result of pathogenic bacteria that may cause systemic symptomsor urinary tract infections. On the other hand, chronicprostatitis/chronic pelvic pain syndrome does not have a clearly definedetiology, and there are many theories about the cause of this disease.

Perhaps the most comprehensive or encompassing theory of chronicnon-bacterial prostatitis is one which advocates a multifactorialmechanism initiated by a stimulus such as infection or trauma. Aninterrelated cascade of events may follow, including physical, chemical,immunologic or neurogenic components, resulting in a local response ofinflammation and/or neurogenic injury.

In the absence of consistent or clear etiologies for chronicprostatitis/chronic pelvic pain syndrome, improvement in quality of lifeand a reduction in symptoms are the usual goals of therapy. The mostcommon treatment for chronic prostatitis involves pharmacologictreatments such as antibiotics, anti-inflammatory agents, alphablockers, anti-spasmodics, analgesics, allopurinol, and musclerelaxants. Alpha blockers have successfully treated symptoms ofprostatitis, although adverse event rates have been high. Musclerelaxants have shown significant improvement in small studies forcategory IIIB patients with sphincter dyssynergia or muscle spasm.Anti-inflammatory agents, such as pentosan polysulfate, have provensuccessful for approximately 40% of patients with category IIIAprostatitis.

Phytotherapeutic agents have demonstrated improvements in small studiesfor pain and irritative voiding. Other treatments include physiotherapy(such as biofeedback and pelvic muscle exercises) and various modalitiesof invasive and minimally invasive procedures (e.g., transurethralmicrowave therapy, transurethral incision of the bladder neck,hydrodistensions, acupuncture, electroneuromodulation, balloon dilation,YAG laser therapy and heat therapy). Repetitive prostatic massage is apopular treatment method due to the failure of consistent standardmedical therapy to treat the condition. Lifestyle changes, such asmeditation, discontinuation of bike riding, sitz-baths, dietary changesand chiropractic therapy, are often prescribed.

As a result of unknown etiology, unsure diagnosis and treatment optionsthat are often myriad and ineffective, chronic prostatitis is a“diagnosis of exclusion” and has a poor record of treatment success.Accordingly, the present invention is intended to provide solutions tothe foregoing problems through improved and more effective methods oftreating pain and other symptoms associated with chronic prostatitis,prostatalgia and prostatodynia.

Sexual dysfunction comprises a broad range of maladies, includingerectile dysfunction, orgasmic dysfunction, premature ejaculation andlack of lubrication. Sexual dysfunctions plague both women and men, andmay be life-long or acquired. To treat impotence (also called erectiledysfunction), electrical conductors may be implanted near the surface ofthe pelvic splanchnic nerve. Stimulation of this nerve with low voltageelectrical pulses is believed to cause arterioles dilation and initiateerection. Also, it is known that implantation of an electrode on thecavernous nerves of a male, adjacent to his prostate gland, may alsocause penile erection. Further, other electrical impulse devices existthat are not implanted but instead apply electrical stimuli topically tothe coccyx region to promote sexual excitation. Impotence, however,should not be confused with orgasmic dysfunction, where satisfactoryerection may be obtained but there is an absence of orgasm.

Current treatment of orgasmic dysfunction concentrates on thepsychological components of the disorder rather than the physiologicalcomponents. Orgasmic dysfunction is a physical malady that results inmarked distress and interpersonal difficulty. The physical disordercauses psychological performance anxiety and pressure. Sexual desire andfrequency usually decline. The patient's intimate relationships usuallysuffer from resentment and conflict. There is anecdotal evidence ofpatients who have experienced mild sensations in the genitalia whileundergoing spinal cord stimulation for pain relief.

Spinal cord stimulation, on the other hand, has been used as a treatmentfor chronic painful conditions for approximately thirty years. Commonly,spinal cord stimulation is used to alleviate pain after failed surgery,pain due to neuropathies, or pain due to inadequate blood flow.Neurostimulation systems have been found to relieve chronic, intractablepain in the limbs or trunk.

The basic concept of neurostimulation as it relates to pain reliefinvolves the substitution of sensations that reach the thalamus of thebrain. Rather than a pain message, the spinal cord stimulation closesthe gate in the spinal cord and replaces the pain sensation with atingling sensation. Electrodes are positioned effectively to createparesthesia in the painful area. Paresthesia refers to a change insensation in an area of the body. Usually paresthesia is used to showchange in neurologic function caused by damage to a nerve or nerves.Paresthesia is usually not an absence of sensation, but a decrease oralteration of sensation. Patients have described paresthesia as a“buzzing sensation.”

Paresthesia is accomplished through the implantation of stimulatingelectrodes within or near the spinal cord. The electrodes are insertedbetween the vertebrae in parallel with the spinal cord. Low-voltageelectrical stimulation is precisely applied to the spinal cord. Throughdirect stimulation of the dorsal column or the targeted peripheralnerve, the sensation of pain is replaced by a more pleasant “tingling”sensation. The sensation may be adjusted in terms of amplitude tocontrol intensity and pulse width to control duration and frequency.Usually such neurostimulation systems are implantable. MedtronicNeurological, a division of Medtronic, Inc. of Minneapolis, Minn., sellsa neurostimulator system used for pain relief. The device has beenapproved by the Federal brug Administration for implantation in thespinal cord to alleviate pain.

One surgical technique to treat urinary control disorders is theimplantable InterStim® therapy, available from Medtronic, Inc., whichapplies mild electrical stimulation to the sacral nerves in the lowerregion of the spine to influence the behavior of structures such as thebladder, sphincter and pelvic floor muscles. Generally, implantation ofthe InterStim system involves surgically implanting a stimulation leadnear the sacral nerves. The stimulation lead is a very small, insulated,electrical conductor with electrical stimulation contacts on the distalend for implantation near the sacral nerves and an electrical connectoron the proximal end of the lead. The lead electrical connector istypically connected to a small extension, and the extension is connectedto a small neurostimulator that operates in a fashion broadly similar tothat of a cardiac pacemaker by delivering occasional small electricalpulses that sometimes create a tingling sensation felt by the patient.The stimulation lead, lead extension and neurostimulator are allimplanted in the patient in a manner that is typically not perceptibleby others. InterStim therapy may improve the condition of a pelvic floordisorder patient and allow the patient to lead a full life. InterStimtherapy is also nondestructive and reversible.

Each year thousands of patients have sacral nerve stimulation systemsimplanted within them for the treatment of urinary incontinence andurinary retention. Therapy success is determined through the evaluationof symptoms related to the disorder. Clinical success for mosttherapies, including sacral nerve stimulation, is defined as a 50%decrease in the following symptoms:

Urge incontinence as measured by:

-   -   Average number of incontinent episodes per day, or    -   Average severity ranking of incontinent episodes, or    -   Average number of absorbent pads or diapers replaced due to        incontinence.

Urinary frequency and urgency as measured by:

-   -   Average number of voids per day, or    -   Average voided volume per void, or    -   Average degree of urgency prior to voiding.

Urinary retention as measured by:

-   -   Decrease in post-void urine residual, or    -   Average number of catheterizations consisting of≧100 ml of        urine, or    -   Average catheter volume per catheterisation (post-void        residual).

Today, electrical stimulation of the sacral nerve is fairly common forthe purpose of treating voiding dysfunction. Although the majority ofpatients receiving sacral nerve stimulation obtain satisfactory reliefof their voiding dysfunction, some patients (less than 50%) do notexperience adequate relief from sacral nerve stimulation techniques ordesire to obtain better results from the therapy.

Electrical stimulation delivered by an intravaginal or a perinealsurface electrode has been shown to inhibit premature and inappropriatedetrusor contractions. The mechanism for such effects appears to derivefrom the electrical stimulation of pudendal nerve afferents (sensoryreceptors or sensory nerve fibers). Input into the pudendal afferentsystem inhibits a parasympathetic reflex loop consisting of bladder wallafferents (sensory reflexes) and efferents (motor reflexes). Thisparasympathetic loop normally senses a distension of the bladder via theafferent limb and responds by sending an efferent signal to contract thebladder. Although such stimulation has shown therapeutic effects,electrode placement and on-going stimulation do not lend themselveseasily to chronic stimulation.

Stimulation of the pudendal nerve as an alternative to sacral nervestimulation has been proposed in past. The invasiveness of the surgicalprocedure for implanting electrical stimulation leads and other reasonshave made stimulation of the pudendal nerve impractical, however. Sincethe pudendal nerve directly innervates much of the pelvic floor, it isbelieved to be a more optimal stimulation site with few undesired sideeffects. Advancements in minimally invasive lead placement techniquesalong with advancement in lead anchoring techniques have resulted in theincreased viability of chronic stimulation of the pudendal nerve.

Some prior art publications relating to various embodiments of thepresent invention are listed in Table 1 below.

TABLE 1 Prior Art Publications Juenemann et al., “Clinical Significanceof Sacral and Pudendal Nerve Anatomy,” The Journal of Urology, Vol. 139,pp. 74-80 (January, 1988). Schmidt, Richard A., “Technique of PudendalNerve Localization for Block or Stimulation, “The Journal of Urology,Vol. 142 (December, 1989). U.S. Pat. No. 4,406,288 to Cash for “BladderControl Device and Method” U.S. Pat. No. 4,607,639 to Tanagho et al. for“Method and System for Controlling Bladder Evacuation.” U.S. Pat. No.4,771,779 to Tanagho et al. for “System for Controlling BladderEvacuation.” U.S. Pat. No. 4,739,764 to Lue et al. for “Method forStimulating Pelvic Floor Muscles for Regulating Pelvic Viscera.” U.S.Pat. No. 4,881,526 to Johnson et al. for “Intravaginal Electrode andStimulation System for Controlling Female Urinary Incontinence” U.S.Pat. No. 5,425,751 to Baeten et al. for “Method and Apparatus forOptimum Positioning of a Muscle Stimulating Implant” U.S. Pat. No.5,540,730 to Terry, Jr. et al. for “Treatment of Motility Disorders byNerve Stimulation” U.S. Pat. No. 5,984,854 to Ishikawa et al. for“Method for Treating Urinary Incontinence and Apparatus Therefor” U.S.Pat. No. 6,055,456 to Gerber for “Single and Multi- Polar ImplantableLead for Sacral Nerve Stimulation” U.S. Pat. No. 6,366,814 to Boveja.for “Electrical Stimulation Adjunct (Add-On) Therapy for UrinaryIncontinence and Urological Disorders Using an External Stimulator” U.S.Pat. No. 6,449,512 to Boveja. for “Apparatus and Method for Treatment ofUrological Disorders Using Programmerless Implantable Pulse GeneratorSystem” U.S. Pat. No. 6,587,719 to Barrett et al. for “Treatment ofObesity by Bilateral Vagus Nerve Stimulation” U.S. Pat. No. 6,609,025 toBarrett et al. for “Treatment of Obesity by Bilateral Sub-DiaphragmaticNerve Stimulation” U.S. Pat. No. patent application publication No.2002/0055761 to Mann et al. for “Implantable Stimulator Systems andMethods for Treatment of Incontinence and Pain” U.S. Pat. No. patentapplication publication No. 2002/0055779 to Andrews for “NeuralProsthesis” PCT patent application WO 02/078592 to Grill et al. for“Systems and Methods for Selectively Stimulating Components In, On orNear the Pudendal Nerve or Its Branches to Achieve Selective PhysiologicResponses” European patent application No. 0 245 547 to Tanagho et al.for “Electronic Control System for Controlling Pelvic Viscera via Neuro-Electrical Stimulation.”

All patents and technical papers listed in Table 1 hereinabove arehereby incorporated by reference herein, each in its respectiveentirety. As those of ordinary skill in the art will appreciate readilyupon reading the Summary of the Invention, Detailed Description of thePreferred Embodiments and Claims set forth below, at least some of thedevices and methods disclosed in the patents and publications of Table 1may be modified advantageously in accordance with the teachings of thepresent invention. The foregoing and other objects, features andadvantages, which will now become more readily apparent by referring tothe following specification, drawings and claims, are provided by thevarious embodiments of the present invention.

SUMMARY OF THE INVENTION

Simultaneous, concurrent or sequential electrical stimulation of anddrug delivery to the left and right pudendal nerves has been discoveredto provide a means of more directly or effectively treating variouspelvic floor disorders than has been possible heretofore through meansof employing conventional therapeutic techniques. Various combinationsand permutations of pudendal nerve or nerve portion electricalstimulation and the delivery of one or more drugs to a tissue volume inproximity to a pudendal nerve or nerve portion, provide particularlyefficacious means of delivering therapies for a number of differentpelvic floor disorders.

It has been discovered that electrical stimulation of the pudendalnerves and/or portions thereof, in combination with the infusion of oneor more drugs to or near at least one target tissue volume in proximityto at least one of such nerves or nerve portions, where the drugs areprovided to or near such a target tissue volume by one or moreimplantable drug delivery devices, provides beneficial effects andtherapies for various disorders of the pelvic floor over a wideranatomical region than merely electrically stimulating the pudendal orsacral nerves or portions thereof, or than may be attained throughconventional sacral nerve stimulation. Because the present inventionprovides for more targeted electrical stimulation of the pelvic floor orportions thereof in combination with the targeted delivery of drugs, atleast some of the undesirable side effects of sacral nerve stimulationmay be avoided or minimized.

One or more electrical stimulation signals are applied, and one or moredrugs are infused, injected or otherwise administered, to appropriateportions of a patient's pelvic floor and the left and right pudendalnerves or nerve portions in an amount and manner effective to treat anumber of disorders, including, but not limited to, urinary and/or fecalvoiding dysfunctions such as constipation, incontinence disorders suchas urge frequency and urinary retention disorders, sexual dysfunctionssuch as orgasmic and erectile dysfunction, pelvic pain, prostatitis,prostatalgia and prostatodynia. Electrical stimulation parameters anddrug type and dosage are tailored to deliver the most efficacioustherapy for a given malady.

At least one electrical stimulation signal is applied by an IMD that hasat least one medical electrical lead positionable, secured or attachedto or in a patient's pelvic floor and in proximity to a pudendal nerveor nerve portion. Each such lead carries at least one electrode, andpreferably at least two electrodes, positionable or attachable forcontact with or in proximity to the patient's pudendal nerves or nerveportions.

Various embodiments of the present invention are capable of providingone or more solutions to one or more problems existing in the prior artrespecting conventional treatment for urinary and/or fecal voidingdysfunctions such as constipation, incontinence disorders such as urgefrequency and urinary retention disorders, sexual dysfunctions such asorgasmic and erectile dysfunction, pelvic pain, prostatitis,prostatalgia and prostatodynia.

Such problems include, but are not limited to, one or more of: (a)sequelae or side-effects resulting from the oral administration ofpharmaceutical products; (b) the requirement to purchase expensivepharmaceutical products on an on-going basis; (c) not having the abilityto terminate or change instantaneously administration of pharmaceuticaltherapy; (d) not having the ability to target with a great deal ofprecision or specificity the ailment in question using orally deliveredpharmaceutical products; (e) in the case of electrical stimulation, nothaving a well-defined or reliable method of determining stimulationelectrode placement; (f) patients having chronic and essentiallyuntreatable pain having no effective pain relief therapy available foruse; (g) patients having to wear diapers, pads or other devices forcontaining human waste, and/or (h) conventional sacral nerve stimulationtechniques being incapable of providing the desired relief or therapy inmany patients.

Various embodiments of the present invention are capable of providingone or more advantages, which may include, but are not necessarilylimited to: (a) targeting the delivery of therapies with a high degreeof specificity; (b) having the ability to change the therapy deliveredon-demand or instantaneously; (c) lowering medical care costs in respectof pharmaceutical products; (d) having the potential to deliverysuperior therapy; (e) a patient not having to remember to take a drugdaily or according to a predetermined regimen; (f) permittingstimulation lead implantation surgical procedures to be completed morequickly; (d) reducing trauma or damage to a patient's pelvic flooranatomy; and/or (g) improved physical and electrical coupling of one ormore stimulation electrodes to a pertinent nerve or nerve portion.

BRIEF DESCRIPTIONS OF THE DRAWINGS

These and other features and advantages of the present invention will bemore readily understood by referring to the following detaileddescription of the preferred embodiments thereof, when considered inconjunction with the drawings, in which like reference numerals indicateidentical structures throughout the several views when appropriate. Notethat the drawings are not necessarily to scale.

FIG. 1 shows one embodiment of the present invention, where INS 10 is acombination implantable pulse generator and drug pump implanted in anupper buttock position in a patient, lead 18 is implanted near oradjacent to pudendal nerve or nerve portion 26, and drug deliverycatheter 300 is implanted near or adjacent to sacral nerve or nerveportion 25, to thereby effect therapeutic relief;

FIG. 2 shows a block diagram illustrating some of the constituentcomponents of INS 10 in accordance with one embodiment of the presentinvention illustrated in FIG. 1;

FIG. 3 shows a simplified anatomical view of portions of the pelvicfloor of a human patient, the locations of sacral and associated nervestherein, and illustrative positionings of INS 10, drug pump or deliverydevice 310, electrical stimulation lead 16 and corresponding electrodes20-23, and drug delivery catheter 300;

FIG. 4 shows a simplified anatomical view of the pelvic floor of afemale human patient, the locations of the left and right pudendalnerves 26 and 27 and associated nerves therein, the positioning of drugpump or delivery device 310, and the positioning of drug deliverycatheters 300 and 301 such that the distal portions thereof are locatednear left and right pudendal nerves 26 and 27;

FIG. 5 shows a simplified male anatomical view of the pelvic floor andthe locations of the pudendal, sacral and associated nerves therein;

FIG. 6 shows a simplified anatomical view of the pelvic floor of afemale human patient, the locations of the sacral nerves 25 andassociated nerves therein, the positioning of drug pump or deliverydevice 310, and the positioning of drug delivery catheter 300 such thatthe distal portion thereof is located near one or more sacral nerves ornerve portions 25;

FIG. 7 shows a simplified anatomical view of portions of the pelvicfloor of a male human patient, the locations of pudendal and associatednerves 26, the locations of sacral and associated nerves 25, andillustrative positionings of INS 10, electrical stimulation lead 16 andcorresponding electrodes 20-23, drug pump or delivery device 310, anddrug delivery catheter 300;

FIGS. 8A through 8E show various embodiments of the distal end of leads16 and 18 of the present invention;

FIG. 9 shows a flow diagram according to one embodiment of a method ofthe present invention for electrically stimulating at least one of thepudendal and sacral nerves, in combination with delivering one or moredrugs to at least one of a sacral nerve 25 and a pudendal nerve 26,associated nerves or portions thereof;

FIGS. 10A through 10F show various embodiments of first and secondelectrical stimulation pulse regimes of the present invention; and

FIGS. 11A through 11G show various embodiments of first and secondelectrical stimulation pulse regimes and first and second drug deliveryregimes of the present invention.

DETAILED DESCRIPTIONS OF THE PREFERRED EMBODIMENTS

In the following description of the preferred embodiments, reference ismade to the accompanying drawings that form a part hereof, and in whichare shown by way of illustration several specific embodiments of theinvention. It is to be understood that other embodiments of the presentinvention are contemplated and may be made without departing from thescope or spirit of the present invention. The following detaileddescription, therefore, is not to be taken in a limiting sense. Instead,the scope of the present invention is to be defined in accordance withthe appended claims. As employed herein, the term “sacral nerve 25”means any one of the sacral nerves, portions of the sacral nerve(s),nerves neurologically connected to any one of the sacral nerves and inrelatively close physical proximity thereto, and extensions or branchesof any one of the sacral nerves. As employed herein, the term “pudendalnerve 26” means the pudendal nerve itself, portions of the pudendalnerve, nerves neurologically connected to the pudendal nerve and inrelatively close physical proximity thereto, and extensions or branchesof the pudendal nerve. Additionally, the term “INS 10” as employedherein is not necessarily limited to meaning an “implantableneurological stimulator” only, but may also mean, depending upon thecontext in which it is used, a combination implantable neurologicalstimulator and drug pump or drug delivery device.

Augmentation of sacral nerve stimulation with pudendal nerve stimulationand/or targeted drug delivery to a target tissue volume is capable ofproviding certain advantages and may help the patient achieve betterclinical outcomes. For example, the nerve integrity of some patients maybe compromised due to the progression of a neurological disease such asmultiple sclerosis or Parkinson's disease. Other patients may havecompromised nerves due to injury caused by obstetrics or accidents. Inthe case of a compromised neurological system in the pelvic floor,signal conduction may be a major issue and a factor in theirincontinence. Because the pelvic floor is innervated by nerve fibersfrom each of the sacral nerves, stimulation of a single sacral nervedoes not always give adequate or full relief of the patient'sincontinence.

Stimulation of and/or drug delivery to both the sacral nerve and thepudendal nerve provides broader electrical stimulation and drug infusionpatterns covering more of the pelvic floor and may result in additionalrelief of the incontinence symptoms. In addition to the sacral nerves,the pudendal and other nerves described herein are good sites tostimulate and/or deliver drugs to because they innervate much of thepelvic floor, including the urinary sphincters.

The sacral nerves innervate the pelvic floor and the legs and feet.Stimulation of the sacral nerve results in stimulation of both thepelvic floor and the leg and foot. One issue that many sacral nervestimulation patients experience is an annoying stimulation of the legand/or foot, which at times may be mitigated through reducing thestimulation level on the sacral nerve. An advantage to stimulating boththe sacral nerve and the pudendal nerve is that lower stimulation levelsmay be used to achieve the same or better therapeutic results which mayeliminate the annoying stimulation of the leg and/or foot. The lowerstimulation levels can result in less sensory stimulation and in thepatient being less aware of the presence of the stimulation. Anadditional advantage is that lower electrical stimulation levelsincrease the life of the battery powering the implanted pulse generator.

According to one embodiment of the present invention, electricalinnervation of and/or drug delivery to the sacral nerves and/or thepudendal nerves is lateralized. That is, electrical stimulation ofand/or drug delivery to the sacral and/or pudendal nerves occurs onopposite sides. For example, the sacral nerve may be electricallystimulated on the left side while a drug is delivered to the pudendalnerve on the right side. The amount and degree of nerve laterilizationis preferably determined by looking to factors such as nerve EMGresponse, anatomical access, physician preference and patientpreference.

FIG. 1 shows one embodiment of the present invention, where INS 10 is acombination implantable pulse generator and drug pump implanted in anupper buttock position in a patient, lead 18 is implanted near oradjacent to pudendal nerve or nerve portion 26, and drug deliverycatheter 300 is implanted near or adjacent to sacral nerve or nerveportion 25, to thereby effect therapeutic relief. Hermetically sealedenclosure 14 is preferably formed of a biocompatible material such as anappropriate metal alloy containing titanium. In addition to housingcircuitry for effecting electrical stimulation of the pelvic floor, INS10 of FIG. 1 also contains circuitry and mechanisms for holding one ormore drugs in a reservoir and delivering such drugs to a target tissuevolume via drug catheter 300.

FIG. 1 shows the distal end of lead 18 implanted near or adjacent topudendal nerve or nerve portion 26, and the distal end of drug catheter300 implanted near or adjacent to sacral nerve 25 or a sacral nerveportion, to thereby effect therapeutic relief. Note, however, that INS10 may be implanted in any appropriate location in the patient, such asin the abdomen or side. Note further that the positions of the distalends of catheter 300 and lead 18 may be exchanged such that a drug isdelivered in close proximity to pudendal nerve or nerve portion 26 whilesacral nerve 25 is electrically stimulated.

Relief is effected by INS 10 and lead 18 as a result of electricalstimulation signals being delivered to or near sacral nerve 25 or nerveportion 8 by electrodes 40-43, and to or near pudendal nerve 26 or nerveportion 8 by electrodes 40-43, as well as by one or more drugs beingdelivered to the distal end of catheter 300, the target tissue volume inproximity to the distal end of drug catheter 300 being infused with suchdrugs through the action of the drug pump component of INS 10/drug pump314.

One, two, three, four or more electrodes 40, 41, 42 and 43 may bedisposed at the distal end of lead 18. FIG. 1 shows four electrodeslocated at the distal end of lead 18 near pudendal nerve 26. Other leadlocations, electrode configurations and lead configurations are possibleand contemplated in the present invention.

Drug catheter 300 may possess more than one port at or near the distalend thereof for the infusion of drugs into a tissue volume in proximityto such port. Indeed, such ports may be disposed anywhere along thelength of catheter 300 according to the requirements at hand and thedisease being treated. Drug catheter 300 may be formed from any of manydifferent, well-known, suitable biocompatible materials, suchpolyurethane, and may contain one, two, three or more lumens disposedtherewithin for carrying drugs to the ports and catheter locationsassociated therewith.

In one embodiment of the present invention, lead 18 provides electricalstimulation pulses to the desired nerve target site or portion 26 andthereby stimulates the target nerve or nerve portion located in thevicinity of the electrode(s) thereof. Lead 18 may have unipolarelectrodes disposed thereon (where enclosure 14 is employed as anindifferent electrode) or may have bipolar electrodes disposed thereon,where one or more electrodes disposed on a lead are employed as theindifferent electrode. In one embodiment of the present invention, Lead18 extends from lead connector 13, which in turn forms an integralportion of lead extension 15 connected at its proximal end to connectorheader module 12.

Typically, catheter 300 and lead 18 are tunneled subcutaneously betweenthe location of INS 10 and the location or site of the nerve or nerveportion 26 that is to be stimulated. INS 10 is typically implanted in asubcutaneous pocket formed beneath the patient's skin according tomethods well known in the art. Further details concerning variousmethods of implanting INS 10 and lead and 18 are disclosed in theMedtronic Interstim Therapy Reference Guide published in 1999, theentirety of which is hereby incorporated by reference herein. Otherknown methods of implanting and locating catheter 300 and lead 18 are ofcourse contemplated in the present invention.

Some representative examples of lead 18 include MEDTRONIC nervestimulation lead model numbers 3080, 3086, 3092, 3487, 3966 and 4350 asdescribed in the MEDTRONIC Instruction for Use Manuals thereof, allhereby incorporated by reference herein, each in its respectiveentirety. Some representative examples of INS 10 include MEDTRONICimplantable electrical stimulator model numbers 3023, 7424, 7425 and7427 as described in the Instructions for Use Manuals thereof, allhereby incorporated by reference herein, each in its respectiveentirety. INS 10 may also be constructed or operate in accordance withat least some portions of the implantable stimulators disclosed in U.S.Pat. No. 5,199,428 to Obel et al., U.S. Pat. No. 5,207,218 to Carpentieret al. or U.S. Pat. No. 5,330,507 to Schwartz, all of which are herebyincorporated by reference herein, each in its respective entirety.

U.S. patent application Ser. No. 10/004,732 entitled “ImplantableMedical Electrical Stimulation Lead Fixation Method and Apparatus” andSer. No. 09/713,598 entitled “Minimally Invasive Apparatus forImplanting a Sacral Stimulation Lead ” to Mamo et al., the respectiveentireties of which are hereby incorporated by reference herein,describe methods of percutaneously introducing lead 18 to a desirednerve stimulation site in a patient.

Certain aspects of the subject matter described in U.S. ProvisionalPatent Application Ser. No. 60/459,077 entitled “Method, System andDevice for Treating Disorders of the Pelvic Floor by means of ElectricalStimulation of the Pudendal and Associated Nerves, and the OptionalDelivery of Drugs in association”, the entirety of which is herebyincorporated by reference herein, where various methods of positioningand implanting a medical electrical lead 18 so as to provide optimalstimulation of the pudendal nerve 26 or a portion thereof, may beadapted for use in conjunction with at least some embodiments of thepresent invention.

FIG. 2 shows a block diagram illustrating some of the constituentcomponents of INS 10 in accordance with one embodiment of the presentinvention, where INS 10 is a combined implantable electrical stimulatorand drug pump having a microprocessor- or controller-based architecture.Other architectures of INS 10 are of course contemplated in the presentinvention, such as the logic or state machine architecture employed inthe Medtronic Model Number 3023 INS. For the sake of convenience, INS 10in FIG. 2 is shown with one catheter 300 and one 18 connected thereto;similar circuitry and connections not shown in FIG. 2 apply generally toother possible additional leads and catheters not shown in the drawings.

INS 10 may be an open-loop non-feedback-control system, or a closed-loopfeedback control system. In the case of a closed-loop feedback controlembodiment of the present invention, FIG. 2 shows optional inputamplifier 97 connected to sensing electrodes 45 and 46 through capacitor99. Similarly, feedback sensors may be employed to control the deliveryof drugs to the patient from drug pump portion 313.

In the embodiment of the present invention shown in FIG. 2, drug pumpportion 313 in FIG. 2 comprises drug reservoir 302, safety valve 303 andpump 304. The proximal end of outlet catheter 300 is connected to drugpump 304. Outlet catheter 300 has a discharge port located at the distalend thereof, which is located in proximity to a tissue volume intendedto be treated with the drug disposed in reservoir 302. In accordancewith well-known methods and devices known in the art, needle 306 isemployed to refill reservoir 302 through an inlet port connected toreservoir 302. Note that drug pump portion 313 may contain multiplereservoirs, safety valves, pumps, and outlet catheters. Digitalcontroller/timer circuit 74 and micro-computer circuit 58 control theoperation of drug pump portion 313, most preferably according toparticularized instructions programmed within micro-computer circuit 58by a health care provider. In some embodiments of the present invention,one or more drugs are dispensed through catheter 300 upon receiving apatient-activated command. Micro-computer 58 is preferably programmed bya health care provider to lock out patient-activated commands that occurduring periods of time when drugs should not be dispensed.

INS 10 in FIG. 2 is most preferably programmable by means of externalprogramming unit 11. One such programmer is the commercially availableMedtronic Model No. 7432 programmer, which is microprocessor-based andprovides a series of encoded signals to INS 10, typically through aprogramming head which transmits or telemeters radio-frequency (RF)encoded signals to INS 10. Another suitable programmer is thecommercially available Medtronic Model No. 8840 programmer, which isalso microprocessor-based but features a touch control screen. Any of anumber of suitable programming and telemetry methodologies known in theart may be employed so long as the desired information is transmitted toand from the implantable electrical stimulator 10.

As shown in FIG. 2, lead 18 is coupled to a node in INS 10 throughcapacitor 98. Microcomputer circuit 58 preferably comprises on-boardcircuit 60 and off-board circuit 62. By way of example, circuit 58 maycorrespond to a microcomputer circuit disclosed in U.S. Patent No. U.S.Pat. No. 5,312,453 to Shelton et al., hereby incorporated by referenceherein in its entirety. On-board circuit 60 preferably includesmicroprocessor 64, system clock circuit 66 and on-board RAM 68 and ROM70. Off-board circuit 62 preferably comprises a RAM/ROM unit. On-boardcircuit 60 and off-board circuit 62 are each coupled by datacommunication bus 72 to digital controller/timer circuit 74.Microcomputer circuit 58 may comprise a custom integrated circuit deviceaugmented by standard RAM/ROM components.

Electrical components shown in FIG. 2 are powered by an appropriateimplantable primary (i.e., non-rechargeable) battery power source 76 orsecondary (i.e., rechargeable) battery power source 76. For the sake ofclarity, the coupling of battery 76 to the various components of INS 10is not shown in FIG. 2. Antenna 56 is connected to microcomputer circuit58 via digital controller/timer circuit 74 and data communication bus 72to permit uplink/downlink telemetry through RF transmitter and receivertelemetry unit 78. By way of example, telemetry unit 78 may correspondto that disclosed in U.S. Pat. No. 4,566,063 issued to Thompson et al.It is generally preferred that the particular programming and telemetryscheme selected permit the entry and storage of electrical stimulationparameters. The specific embodiments of antenna 56 and other telemetrycircuitry presented herein are shown for illustrative purposes only, andare not intended to limit the scope of the present invention.

Continuing to refer to FIG. 2, V_(REF) and bias circuit 82 mostpreferably generate stable voltage reference and bias currents foranalog circuits included in output circuit 54. Operating commands forcontrolling the timing of INS 10 are coupled by data bus 72 to digitalcontroller/timer circuit 74, where digital timers and counters establishthe specific stimulation parameters of INS 10 as well as various timingwindows for controlling the operation of peripheral components disposedwithin input/output circuit 54. Output pulse generator 96 provideselectrical stimuli to desired nerve and/or nerve portion 25 or 26through coupling capacitor 98 in response to a trigger signal providedby digital controller/timer circuit 74, when an externally transmittedstimulation command is received, or when a response to other storedcommands is received.

By way of example, output amplifier 96 may correspond generally to anoutput amplifier disclosed in U.S. Patent No. U.S. Pat. No. 4,476,868 toThompson, hereby incorporated by reference herein in its entirety. Thespecific embodiments of output amplifier 96 identified herein arepresented for illustrative purposes only, and are not intended to belimiting in respect of the scope of the present invention. The specificembodiments of such circuits may not be critical to practicing someembodiments of the present invention so long as they provide means forgenerating an appropriate train of stimulating pulses to desired nerveor nerve portion 25 and/or 26.

In various embodiments of the present invention, INS 10 may beprogrammably configured to operate so that it varies the rate at whichit delivers stimulating pulses to desired nerve or nerve portion 25and/or 26, and/or to vary the rate or manner at which outlet catheter300 delivers one or more drugs to a desired tissue volume, in responseto one or more selected outputs being generated, or in response to oneor more signals of interest being detected by one or more sensors. INS10 may further be programmably configured to operate so that it may varythe morphology of the stimulating electrical and/or drug output pulsesit delivers. Numerous implantable electrical stimulator features andfunctions not explicitly mentioned herein may be incorporated into INS10 while remaining within the scope of the present invention. Variousembodiments of the present invention may be practiced in conjunctionwith one, two, three or more leads, in conjunction with one, two, three,four or more electrodes disposed on each lead, or in conjunction withone, two, three or more outlet catheters connected thereto.

Leadless embodiments of the present invention are also contemplated,where one or more electrical stimulation, drug pump or other type ofdrug delivery device, and/or sensing electrode capsules or modules areimplanted at or near a desired nerve or nerve portion 25 and/or 26, andthe capsules or modules deliver electrical stimuli or drugs directly tothe selected site using a preprogrammed stimulation or drug deliveryregime, and/or the capsules or modules sense electrical, chemical orother pertinent signals for monitoring and feedback control purposes.Such capsules or modules are preferably powered by rechargeablebatteries that may be recharged by an external battery charger usingwell-known inductive coil or antenna recharging means, and preferablycontain electronic circuitry sufficient to permit telemetriccommunication with a programmer, to deliver electrical stimuli and/orsense electrical or other signals, and to store and execute instructionsor data received from the programmer. Alternatively, in one embodimentof the present invention INS 10 is configured to recharge such aremotely positioned capsule or module by RF means on a periodic basisaccording to battery state of charge requirements measured or exhibitedby such remote capsule or module.

Examples of methods and devices that may be adapted for use in thewireless devices and methods of the present invention include thosedescribed in U.S. Pat. No. 6,208,894 to Schulman et al. entitled “Systemof implantable devices for monitoring and/or affecting body parameters;”U.S. Pat. No. 5,876,425 to Schulman et al. entitled “Power control loopfor implantable tissue stimulator;” U.S. Pat. No. 5,957,958 to Schulmanet al. entitled “Implantable electrode arrays;” U.S. patent applicationSer. No. 09/030,106 filed Feb. 25, 1998 to Schulman et al. entitled“Battery-Powered Patient Implantable Device,” and U.S. Pat. No.6,650,943 to Whitehurst et al. entitled “Fully ImplantableNeurostimulator for Cavernous Nerve Stimulation as a Therapy forErectile Dysfunction and Other Sexual Dysfunction.”

FIG. 3 shows a simplified anatomical view of portions of the pelvicfloor of a human patient, the locations of sacral and associated nervestherein, and illustrative positionings of INS 10, drug pump or deliverydevice 310, electrical stimulation lead 16, corresponding electrodes20-23, and drug delivery catheter 300. FIG. 3 shows INS 10 implanted inan appropriate location within the patient, with lead 16 being implantednear or adjacent to one or more of sacral nerves S1, S2, S3, and/or S4,and the distal end of outlet catheter implanted near or adjacent tosacral nerve or nerve portion 25 to thereby effect therapeutic relief.Such relief is effected as a result of electrical stimulation signalsand drugs being delivered to or near to or near one or more of suchnerves S1, S2, S3 25, S4, and/or pudendal nerve or nerve portion 26, ora nerve(s) in proximity thereto, by electrodes 20, 21, 22, and/or 23 andoutlet catheter 300. One, two, three, four or more electrodes 20, 21, 22and 23 may be disposed at the distal end of lead 16. A second electricalstimulation lead 18, not shown in FIG. 2, having one, two, three, fouror more electrodes 40, 41, 42 and 43 may be employed to electricallystimulate nerve or nerve portion 25 or 26, according to the particularrequirements at hand. Consistent with the foregoing description, otherlead locations, electrode configurations and outlet catheterconfigurations are of course possible and contemplated in the presentinvention.

FIG. 4 shows a simplified anatomical view of the pelvic floor of afemale human patient, the locations of the left and right pudendalnerves 26 and 27 and associated nerves therein, the positioning of drugpump or delivery device 310, and the positioning of drug deliverycatheters 300 and 301 such that the distal portions thereof are locatednear left and right pudendal nerves 26 and 27. Note that the distal endsof drug delivery or outlet catheters 300 and 301 may also be locatednear sacral nerve(s) or nerve portion(s) 25, and that variouspermutations and combinations of locations near or at pudendal nerves ornerve portions 26 and sacral nerve or nerve portions 25 are alsocontemplated in the present invention.

As shown in FIG. 4, pudendal nerve or nerve portion 26 innervates thepelvic floor muscle and sphincters. FIG. 4 shows INS 10 implanted in anappropriate location within the patient, with drug delivery catheters300 and 301 being implanted near or adjacent to one or more of leftpudendal nerve or nerve portion 26 and right pudendal nerve or nerveportion 27, to thereby effect therapeutic relief. Such relief iseffected as a result of an appropriate amount of drug being delivered tothe desired tissue volume(s) according to an appropriate schedule timeregime, where such tissue volumes are in proximity to the desired nerveor nerve portion. Consistent with the foregoing description, other drugdelivery catheter locations and configurations are of course possibleand contemplated in the present invention.

FIG. 5 shows a simplified male anatomical view of the pelvic floor andthe locations of pudendal nerve 26 and nerves associated therewith,where in accordance with some embodiments of the present invention leads16 and/or 18, electrodes 20-23 and/or 40-43, and drug delivery catheters300 and 301 may be attached, connected or implanted in proximitythereto. Pudendal nerve 26 may be seen to extend downwardly pastsacrospinal ligament 43, greater sciatic foramen 48, and lesser sciaticforamen 49, and thereafter to branch into inferior rectal nerves 51,perineal nerves 52, scrotal nerves 53 and dorsal nerve 55 of penis 35.

FIG. 6 shows a simplified anatomical view of the pelvic floor of afemale human patient, the locations of the sacral nerves and nerveportions 25 and associated nerves therein, the positioning of drug pumpor delivery device 310, and the positioning of drug delivery catheter300 such that the distal portion thereof is located near one or moresacral nerves or nerve portions 25. Other sites or tissue volumes towhich one or more drugs may be delivered by drug pump 300 and drugdelivery catheter 301 are also illustrated in FIG. 6, such as the lessersplanchnic nerve or nerve portion, the least splanchnic nerve or nerveportion, the sympathetic trunk nerve or nerve portion, the lumbarsplanchnic nerve or nerve portion, the L1, L2, L3, L4, etc, spinal nerveor nerve portion, the ovarian plexus, aorticorneal ganglia, the superiormesenteric ganglion, the intermesenteric (aortic) plexus, the superiorhypogastric nerves or nerve portions, the uterovaginal plexus, theinferior hypogastric plexus, one or more of the pelvic splanchnic nervesor nerve portions.

FIG. 7 shows a simplified anatomical view of portions of the pelvicfloor of a male human patient, the locations of pudendal and associatednerves 26, the locations of sacral and associated nerves 25, andillustrative positionings of INS 10, electrical stimulation lead 18 andcorresponding electrodes 40-43, drug pump or delivery device 310, anddrug delivery catheter 300. in FIG. 7, the distal end of drug deliverycatheter 300 is located near or at the prostatic plexus. Other sites ortissue volumes to which one or more drugs may be delivered by drug pump300 and drug delivery catheter 301 are also illustrated in FIG. 7, suchas the prostate, the bladder, the penis, and the superior hypogastricnerves or nerve portions. Many locations within a patient's body may beelectrically stimulated or infused with one or more drugs in accordancewith various embodiments of the present invention, including, but notlimited to, a sacral nerve or branches or portions thereof, a pudendalnerve or branches or portions thereof, a hypogastric nerve or branchesor portions thereof, a prostatic plexus nerve or branches or portionsthereof, a sacral splanchnic nerve or branches or portions thereof, apelvic splanchnic nerve or branches or portions thereof, the prostate orbranches or portions thereof, the pelvic floor, the colon or branches orportions thereof, the bladder or portions thereof, the vagina orportions thereof, the anus or portions thereof, the external analsphincter or portions thereof, the urethra or portions thereof, thepenile dorsal nerve or portions thereof, inferior rectal nerves orbranches or portions thereof, perineal nerves or branches or portionsthereof, scrotal nerves or branches or portions thereof, the scrotum orportions thereof, Alcock's Canal or branches or portions thereof,sacro-tuberous ligament or branches or portions thereof, ischialtuberosity or branches or portions thereof, greater sciatic foramen orbranches or portions thereof, or lesser sciatic foramen or branches orportions thereof,

FIGS. 8A through 8E show various embodiments of a distal end of medicalelectrical lead 16 and/or 18 of the present invention. In FIG. 8A, lead16/18 is a paddle lead having electrodes 20-23 arranged along anoutwardly facing planar surface. Such a paddle lead 16/18 is preferablyemployed to stimulate peripheral nerves. In FIG. 8B, lead 16/18 is aconventional quadrapolar lead having no pre-attached anchoring mechanism19. Electrodes 20-23 are cylindrical in shape and extend around thecircumference of the lead body.

In FIG. 8C, lead 16/18 is a quadrapolar lead having tined lead anchors19. Tines 19 may be formed from flexible or rigid biocompatiblematerials in accordance with the desired application. Representativeexamples of some tined and other types of leads suitable, adaptable ormodifiable for use in conjunction with the systems, methods and devicesof the present invention include those disclosed in U.S. patentapplication Ser. No. 10/004,732 entitled “Implantable Medical ElectricalStimulation Lead Fixation Method and Apparatus” and Ser. No. 09/713,598entitled “Minimally Invasive Apparatus for Implanting a SacralStimulation Lead ” to Mamo et al., as well as those disclosed in U.S.Pat. No. 3,902,501 to Citron entitled “Endocardial Lead,”U.S. Pat. No.4,106,512 to Bisping entitled “Transvenously Implantable Lead,” U.S.Pat. No. 5,300,107 to Stokes entitled “Universal Tined Myocardial PacingLead.”

In FIG. 8D, lead 16/18 is a quadrapolar lead having pre-attached sutureanchor 19. In FIG. 8E, lead 16/18 is a tri-polar cuff electrode, wherecuff/anchor 19 is wrapped around desired nerve or nerve portion 8 tothereby secure the distal end of lead 16/18 to the nerve and positionelectrodes 20-22 against or near nerve or nerve portion 25 or 26. TheMedtronic Model No. 3995 cuff electrode lead is one example of a leadthat may be adapted for use in the present invention, the Instructionsfor Use manual of which is hereby incorporated by reference herein inits entirety.

Leads 16 and 18 are preferably less than about 5 mm in diameter, andmost preferably less than about 1.5 mm in diameter. Polyurethane is apreferred material for forming the lead body of leads 16 and 18,although other materials such as silicone may be employed. Electricalconductors extending between the proximal and distal ends of leads 16and 18 for supplying electrical current to the electrodes are preferablyformed of coiled, braided or stranded wires comprising an MP35Nplatinum-iridium alloy. Electrodes 20, 21, 22 and 23 and 40, 41, 42 and43 may be ring electrodes, coiled electrodes, electrodes formed fromportions of wire, barbs, hooks, spherically-shaped members,helically-shaped members, or may assume any of a number of differentstructural configurations well known in the art.

Inter-electrode distances on leads 16 and 18 are preferably about 3 mm,but other inter-electrode distances may be employed such as about 1 mm,about 2 mm, about 4 mm, about 5 mm, about 6 mm, about 7 mm, about 8 mm,about 9 mm, about 10 mm, about 12 mm, about 14 mm, about 16 mm, about 18mm, about 20 mm, about 25 mm, about 30 mm.

Preferred surface areas of electrodes 20, 21, 22 and 23 and 40, 41, 42and 43 range between about 1.0 sq. mm and about 100 sq. mm, betweenabout 2.0 sq. mm and about 50 sq. mm, and about 4.0 sq. mm and about 25sq. mm.

Preferred lengths of electrodes 20, 21, 22 and 23 and 40, 41, 42 and 43range between about 0.25 mm and about 10 mm, between about 0.50 mm andabout 8 mm, and about 1 mm and about 6 mm.

Electrodes 20, 21, 22 and 23 and 40, 41, 42 and 43 are preferably formedof platinum, although other metals and metal alloys may be employed suchas stainless steel or gold.

The distal portion of lead 16 extends to a target site or position neara desired nerve or nerve portion 25 and/or 26, and is preferably held insuch position by lead anchor 19. Note that lead anchor 19 may assume anyof a number of different structural configurations such one or moresuture sleeves, cuffs, tines, barbs, hooks, helical screws, tissuein-growth mechanisms, adhesive, polycyanoacrylate, or glue.

One, two, three, four or more electrodes 20, 21, 22 and 23 or 40, 41, 42and 43 may be disposed at the distal end of lead 16 and/or lead 18.Electrodes 20, 21, 22 and 23 and 40, 41, 42 and 43 are preferablyarranged in an axial array, although other types of arrays may beemployed such as inter-lead arrays of electrodes between the distal endsof leads 16 and 18 such that nerves or nerve portions 8 disposed betweenleads 16 and 18 may be stimulated.

Leads 16 and 18 preferably range between about 4 inches and about 20inches in length, and more particularly may be about 6 inches, about 8inches, about 10 inches, about 12 inches, about 14 inches, about 16inches or about 18 inches in length, depending on the location of thesite to be stimulated and the distance of INS 10 from such site. Otherlead lengths such as less than about 4 inches and more than about 20inches are also contemplated in the present invention.

FIG. 9 shows a flow diagram according to one embodiment of a method ofthe present invention for electrically stimulating one or more sacralnerves or nerve portions 25, and infusing one or more drugs to one ormore pudendal nerves or nerve portions 26. Note that the order in whichthe steps shown in FIG. 9 are carried out may be changed, and that theresulting method will nevertheless fall within the scope of the presentinvention. In FIG. 9, at step 110 one or more desired sacral nerveelectrical stimulation locations are located. Various techniques such asvisualization under fluoroscopy or the use of anatomical landmarks maybe used to locate the sacral nerve or nerve portion 25 to be stimulated.Step 120 is employed to test and verify proper sacral nerve or nerveportion 25 response prior to implantation of the stimulation electrode.An electrical signal delivered to the nerve through a needle istypically employed to elicit such a nerve response. The nerve responsemay be detected through a motor response that may be visually detected,a sensory response as reported by the patient or through an electricalresponse. Following verification of proper nerve response, at step 130the sacral nerve electrode is implanted. In step 140, INS 10 having drugpump portion 314 disposed therewithin is implanted in an appropriatelocation within the patient such that the proximal end of lead 16 or 18may be operably connected thereto, and such that INS 10 is placed insuch a location that discomfort and the risk of infection to the patientare minimized.

Step 150 in FIG. 7 is employed to locate the pudendal nerve. Location ofpudendal nerve or nerve portion 26 is typically done through theidentification of anatomical landmarks. Palpation of the patient as wellas usage of fluoroscopy, x-ray and EMG may be employed to assist inproper location of the pudendal nerve. Before or after step 170, INS 10is implanted in an appropriate location within the patient such thatdrug delivery catheter 300 may be operably connected thereto, and suchthat INS 10 is placed in such a location that discomfort and the risk ofinfection to the patient are minimized. Step 180 is used to operablyconnect INS 10 to one or more drug delivery catheters 300, which may ormay not require the use of an optional lead or catheter extension andcatheter connector. In Step 190, INS 10 is activated and stimulationpulses are delivered to electrodes 20, 21, . . . n or 40, 41, . . . nthrough lead 16 or 18 to the desired nerve stimulation location 25 or 26and one or more drugs are delivered via one or more drug deliverycatheters 300 to the desired tissue volume(s). In step 200, electricalpulse stimulation and drug delivery parameters are adjusted to optimizethe therapy delivered to the patient. Such adjustment may entail one ormore of adjusting the number or configuration of electrodes, leadsand/or drug delivery catheters used to stimulate or infuse with drugsthe selected location, pulse amplitude, pulse frequency, pulse width,pulse morphology (e.g., square wave, triangle wave, sinusoid, biphasicpulse, tri-phasic pulse, etc.), times of day or night when pulses ordrugs are delivered, pulse cycling times, the positioning of the lead orleads and/or catheter or catheters, and/or the enablement or disablementof “soft start” or ramp functions respecting the stimulation regime ordrug supply regime to be provided. Note that methods of the presentinvention further contemplate the placement and implantation of multipleelectrical stimulation leads and multiple drug delivery catheters.

FIGS. 10A through 10F shows various embodiments of the first and secondelectrical stimulation pulse regimes of the present invention. In FIG.10A, electrical pulses delivered to a first nerve or nerve portion aresynchronized with the electrical pulses delivered to a second nerve ornerve portion. In FIG. 10B, electrical pulses delivered to a first nerveor nerve portion are out of phase in respect of the electrical pulsesdelivered to a second nerve or nerve portion. In FIG. 10B, theelectrical pulses delivered to the first nerve or nerve portion have alower frequency than the electrical pulses delivered to the second nerveor nerve portion. In FIG. 10D, electrical pulses delivered to a firstnerve or nerve portion are characterized in having different stimulationparameters than those of the electrical pulses delivered to a secondnerve or nerve portion. In FIG. 10E, electrical pulses are deliveredwithout interruption and on a continuous basis to a first nerve or nerveportion, while the delivery of electrical pulses to a second nerve ornerve portion is suspended for a period of time. In FIG. 10F, electricalpulses are delivered to a first nerve or nerve portion and a secondnerve or nerve portion, but at a certain point in time are suspended fora predetermined period of time or until a sensed quantity changes in apredetermined fashion.

Some examples of dual electrical stimulation techniques falling withinthe scope of the present invention are as follows:

-   One pulse regime may be delivered continuously, while the other    pulse regime is turned on and off in accordance with the patient's    symptoms, as such symptoms may wax and wane;-   Both pulse regimes may be delivered continuously, one intermittently    and the other continuously, or both intermittently;-   The two pulse regimes may be different in respect of amplitude,    pulse-width, frequency, pulse morphology, and the like;-   One or both pulse regimes may be delivered according to a scheduled    or detected activity, or according to a predetermined or detected    schedule, the activity or schedule having one or more pulse regimes    associated therewith, the activities or schedules comprising one or    more of circadian rhythms, daytime or nighttime activities or    schedules, meals, periods of exercise, periods of sleep, sexual    activity, and the like;-   One pulse regime may be delivered in accordance with a preprogrammed    regime, while the other pulse regime may be delivered, activated,    modified and/or terminated via patient activation, modification or    termination;-   One or both pulse regimes may be delivered between different leads    having one or more electrodes each to obtain a spatially broad    stimulation pattern;-   One or both pulse regimes may be controlled, activated and/or    terminated by the patient to customize the delivered therapy.

Some representative ranges of preferred electrical pulse stimulationparameters capable of being delivered by INS 10 through leads 16 and/or18 include the following:

Frequency: Between about 50 Hz and about 100 Hz; Between about 10 Hz andabout 250 Hz; and Between about 0.5 Hz and about 500 Hz. Amplitude:Between about 1 Volt and about 10 Volts; Between about 0.5 Volts andabout 20 Volts; and Between about 0.1 Volts and about 50 Volts. PulseWidth: Between about 180 microseconds and about 450 microseconds;Between about 100 microseconds and about 1000 microseconds; and Betweenabout 10 microseconds and about 5000 microseconds.

In the event multiple signals are employed to stimulate a desired site,the spatial and temporal phase between the signals may be adjusted orvaried to produce the desired stimulation pattern or sequence. That is,in the present invention beam forming and specific site targeting viaelectrode array adjustments are specifically contemplated. Electrodeconfigurations, arrays and stimulation patterns and methods similar tothose disclosed by Holsheimer in U.S. Pat. No. 6,421,566 entitled“Selective Dorsal Column Stimulation in SCS, Using Conditioning Pulses,”U.S. Pat. No. 5,643,330 entitled “Multichannel Apparatus for EpiduralSpinal Cord Stimulation” and U.S. Pat. No. 5,501,703 entitled“Multichannel Apparatus for Epidural Spinal Cord Stimulator,” therespective entireties of which are hereby incorporated by referenceherein, may also be adapted or modified for use in the presentinvention. Electrode configurations, arrays, leads, stimulation patternsand methods similar to those disclosed by Thompson in U.S. Pat. No.5,800,465 entitled “System and Method for Multi-site Steering of CardiacStimuli,” the entirety of which is hereby incorporated by referenceherein, may also be adapted or modified for use in the present inventionto permit the steering of electrical fields. Thus, although FIG. 1 showsfour electrodes located at the distal end of lead 16 near sacral nerveS3, other lead locations and electrode configurations are possible andcontemplated in the present invention.

In various embodiments of the present invention it is contemplated thatdrugs be delivered to specific sites within a patient using fullyimplantable or external drug pump devices in combination with providingelectrical stimulation to the nerves or nerve portions described above.According to such devices and methods, and as discussed above, drug pumpportion 314 may be incorporated into the same housing as INS 10 or, iffully implantable, be separate therefrom in its own hermetically sealedhousing. Drug delivery catheter 300 may be attached to drug pump portion314 of INS 10, or may be attached to a separate implantable or externaldrug pump through which one or more drugs are delivered to a specificdesired target tissue volume. Drug delivery catheter 300 may also beincorporated into lead 16 or 18, or may be separate therefrom. Drugs ortherapeutic agents delivered in accordance with this method include, byway of example, antibiotics, pain relief agents such as demerol andmorphine, radioactive or radio-therapeutic substances or agents forkilling or neutralizing maycer cells, genetic growth factors forencouraging the growth of healthy tissues, drugs for facilitating orencouraging penile or clitoral engorgement, and so forth, more aboutwhich we say below.

Drug pumps employed to treat various disease states in accordance withsome embodiments of the present invention may be of the well knownperistaltic type having reservoirs filled with a liquid containing thedrug(s) to be dispensed, or may constitute any of a number of differenttypes of implantable or external drug pump or dispenser types, such asan implantable drug dispenser adapted to deliver drug pellets in solidor semi-solid form to an internal portion of a patient's body atpre-defined intervals. Drug pumps of the present invention may bepowered by primary or rechargeable batteries, and may be communicatedwith or programmed in accordance with telemetry protocols such as thoseemployed in pacemakers or currently marketed implantable drug pumps.

Moreover, in the present invention it is contemplated that drugs bedelivered to one or more target tissue volumes in the vicinity of targetnerves or branches or portions thereof, as well as into other tissues orvoids such as the bladder, one or more smooth muscles, the spinalcolumn, the kidneys, the prostate gland, the testes or testicles, theuterus, the vagina, the penis, the colon, one or more of the pelvicfloor muscles, the vascular system, the intestines, the digestive tract,the stomach, the esophagus, or any of a number of different sphincters(e.g., urethral, anal, etc.) or other muscles or organs.

The following issued U.S. patents, all of which are incorporated byreference herein, each in its respective entirety, describe variousaspects pertaining to different embodiments of the of the drug pumps andcommunication systems of the present invention:

U.S. Pat. No. 4,692,147 to Duggan for “Drug administration device;”

U.S. Pat. No. 4,987,897 to Funke for “Body bus medical devicecommunication system;”

U.S. Pat. No. 5,083,908 to Gagnebin et al. for “Miniature peristalticpump;”

U.S. Pat. No. 5,382,236 to Otto et al. for “Implantable infusion pump;”

U.S. Pat. No. 5,480,656 to Okada et al. for “Prolonged releasemicrocapsules;”

U.S. Pat. No. 5,551,849 to Christensen for “Medication delivery deviceand method of construction;”

U.S. Pat. No. 5,609,575 to Larson et al. for “Infusion pump and methodwith dose-rate calculation;”

U.S. Pat. No. 5,639,275 to Baetge for “Delivery of biologically activemolecules using cells contained in biocompatible immunoisolatorycapsules;”

U.S. Pat. No. 5,683,432 to Goedeke for “Adaptive, performance-optimizingcommunication system for communicating with an implanted medicaldevice;”

U.S. Pat. No. 5,733,313 to Barreras et al. for “RF coupled, implantablemedical device with rechargeable back-up power source;”

U.S. Pat. No. 6,210,368 to Rogers for “Reservoir volume sensors;”

U.S. Pat. No. 6,263,246 to Goedeke for “Method and apparatus forcommunications with an implantable device;”

U.S. Pat. No. 6,283,949 to Roorda for “Refillable implantable drugdelivery pump;”

U.S. Pat. No. 6,322,330 to Thomas for “Compact peristaltic meteringpump;”

U.S. Pat. No. 6,358,202 to Arent for “Network for implanted computerdevices;”

U.S. Pat. No. 6,458,118 to Lent et al. for “Drug delivery throughmicroencapsulation;”

U.S. Pat. No. 6,471,645 to Warkentin for “Communications system for animplantable device and a drug dispenser;”

U.S. Pat. No. 6,485,464 to Christenson et al. for Reduced heightimplantable drug infusion device;”

U.S. Pat. No. 6,551,290 to Elsberry et al. for “Catheter for targetspecific drug delivery;”

U.S. Pat. No. 6,669,663 to Thompson for “Closed loop medicament pump;”

U.S. Pat. No. 6,669,663 to Thompson for “Closed loop medicament pump;”

Tables 1 through 10 below lists drugs that may be employed in variousembodiments of the present invention according to the general diseasestate they are intended to treat (e.g., bladder over-activity or stressincontinence), the effects or actions such drugs promote or cause, theapplicable class(es) of drugs having such effects or actions, the namesof some of the specific drugs falling within the scope of such drugclass(es), and delivery sites for such drugs.

TABLE 1 Drugs for Treatment of Bladder Over-Activity Action Drug ClassSpecific Drug Delivery Site Depress Bladder Antimuscarinic Tolterodine,Digestive system, central Contractions (Anticloinergic) Trospium,nervous system, pudendal Propantheline, nerves, sacral nerves, vascularAtropine, system Hyoscyamine, Darifenacin, Solifenacin Detrusor MuscleMembrane Calcium Digestive system, central Inhibitor channel drugsAntagonists and nervous system, pudendal Potassium nerve, sacral nerves,vascular Channel Openers system Mixed Mode Antimuscarinic andterodiline, Digestive system, central channel blockers oxybuynin,nervous system, pudendal propiverine and nerves, sacral nerves, vascularflaxoxate. system Detrusor Muscle Alpha Alfuzosin, Digestive system,central Relaxant Adrenoceptor Doxazosin, nervous system, pudendalAntagonists Prazosin, nerves, sacral nerves, vascular Terazosin, systemTamsulosin. Detursor Beta Adrenoceptor Terbutaline, Digestive system,central Inhibitor Agonists Chenbuterol, nervous system, pudendalSalbutomol nerves, sacral nerves, vascular system Detursor InhibitorAntidepressants Imipramine. Digestive system, central Blockade ofnervous system, pudendal Reuptake of nerves, sacral nerves, vascularSerotonin and system Noradrenaline Prostatglandin ProstatglandinIndomethacin, Digestive system, central Synthesis SynthesisFlurbiprofen. nervous system, pudendal Inhibitors Inhibitors nerves,sacral nerves, vascular system Motor Neuron Motor Neuron BaclofenDigestive system, central Suppression Supression nervous system,pudendal nerves, sacral nerves, vascular system Sensory SensoryResiniferatoxin, Bladder desensitization Capsaicin Inflammation,Inflammation, pain Dimethyl Sulfox- Bladder Pain, Muscle ide or bacillusContractions Calmette-Guerin (BCG) Hormonal Hormone estrogen Digestivesystem, central treatment nervous system, pudendal nerves, sacralnerves, vascular system

TABLE 2 Drugs for Treatment of Stress Incontinence Action Drug ClassSpecific Drug Delivery Site sphincter and Alpha Ephedrine and Digestivesystem, central urethral muscle Adrenoceptor Norephedrine nervoussystem, Alpha Adrenoceptor Antagonists pudendal nerves, sacralAntagonists nerves, vascular system Control of the Beta AdrenoceptorPropranolol Digestive system, central Urethra Agonists nervous system,pudendal nerves, sacral nerves, vascular system, urethra Contractilityof adrenaline and Imipramine Digestive system, central the Urethraserotonin uptake nervous system, inhibitor pudendal nerves, sacralnerves, vascular system, urethra External Urethral Duloxetine DuloxetineDigestive system, central Sphincter Neural nervous system, ActivityEnhancer pudendal nerves, sacral nerves, vascular system, urethra,urethral sphincter Hormonal Treatment Hormone Estrogen Digestive system,central nervous system, pudendal nerves, sacral nerves, vascular system,pelvic floor, urethra, bladder

TABLE 3 Drugs for Treatment of Overflow Incontinence Action Drug ClassSpecific Drug Delivery Site Increase Bladder Alpha- Alfuzosin, Digestivesystem, central Sensitivity Adrenoceptor Doxazosin, nervous system,Antagonists Prazosin, pudendal nerves, sacral Terazosin, nerves,vascular system, Tamsulosin and bladder Phenoxybenzamine IncreaseBladder Muscarinic Bethanechol, Digestive system, central SensitivityReceptor Carbahol nervous system, Agonists pudendal nerves, sacralnerves, vascular system, bladder Increase Bladder AnticholinesteraseDistigmine Digestive system, central Sensitivity Inhibitors nervoussystem, pudendal nerves, sacral nerves, vascular system, bladderHormonal Treatment Hormone Estrogen Digestive system, central nervoussystem, pudendal nerves, sacral nerves, vascular system, pelvic floor,urethra, bladder

TABLE 4 Interstitial Cystitis Action Drug Class Specific Drug DeliverySite Bacterial antibiotic Flouroquinolones, Digestive system,Elimination Trimethoprimsulfa vascular system, methoxazole prostate Painrelief Analgesic Aspirin, Central nervous acetaminophen, system,pudendal phenazopyridine, nerve, sacral opioid medications nerves suchas meperidine, hydromorphone, methandone, levorphanol, morphine

TABLE 5 Interstitial Cystitis Action Drug Class Specific Drug DeliverySite Bladder Lining Anti-inflammatory Glucosamine, Bladder Healingchondroitin and quercetin combination, hyaluronic acid, pentosanpolysulfate sodium, heparin sodium Pain Relief Analgesic Aspirin,Central nervous system, acetaminophen, pudendal nerve, sacralphenazopyridine, nerves opioid medications such as meperidine,hydromorphone, methandone, levorphanol, morphine Bladder TricyclicAmitriptyline, Bladder, sacral nerves, Antispasmodic antidepressantsdeipramine, pudendal nerves nortriptyline, doxepin, imipramine BladderMuscle relaxant Hyoscyamine, Bladder, pudendal Antispasmodic oxybutyninnerves, sacral nerves, chloride, central nervous system cyclobenzprine,hyoscyamine sulfate, baclofen Urinary Urgency AnticholinergicTolterodine Bladder, pudendal nerve, tartrate sacral nerves, centralnervous system Pain Sensory Resiniferatoxin Bladder desensitizationInflammation, Inflammation, Dimethyl Sulfoxide Bladder Pain, Muscle painor bacillus Contractions Calmette-Guerin (BCG) Aid in Repair of Bladderlining Pentosan Bladder Bladder Lining Polysufate Sodium HormonalHormone estrogen Central nervous system, Treatment pudendal nerves,sacral nerves, vascular system, pelvic floor, urethra, bladder

TABLE 6 Fecal Incontinence/Irritable Bowel Syndrome Action Drug ClassSpecific Drug Delivery Site Diarrhea Anti-diarrheal Loperamide,Digestive tract alosetron Motility Motility inhibition Diphenoxylate,Digestive tract difenoxin, alosetron, cilansetron Motility Motilitystimulation Tagaserod, Digestive Tract cisapride, erythomycin, caffeineIncontinence Tricyclic Amitriptyline Digestive Tract antidepressant

TABLE 7 Female Sexual Dysfunction Action Drug Class Specific DrugDelivery Site Libido, Vaginal Sildenafil Digestive system, Dryness,Sexual vascular system, Nervous Arousal system Libido, Vaginal HormoneEstrogen, Digestive system, Dryness, Sexual Replacement testosteronevascular system Arousal Smooth Muscle Amino acid L-arginine Digestivesystem, Relaxant vascular system Smooth Muscle Smooth MusclePhentolamine Digestive system, Relaxant, Increased Relaxant vascularsystem Vaginal Blood Flow Dopamine Activation Orgasm, libido AmantadineDigestive system, vascular system, central nervous system, deep brainSerotonin Re-uptake Orgasm Bupropion Digestive system, Inhibitorvascular system, central nervous system, deep brain Anti-anxiety Orgasm,Libido Buspione Digestive system, vascular system, central nervoussystem, deep brain Antiserotonergic Orgasm, Libido CypropeptadineDigestive system, vascular system, central nervous system, deep brainSympathomimetic Orgasm Dextroamphetamine Digestive system, vascularsystem, central nervous system, deep brain Sympathomimetic OrgasmPemoline Digestive system, vascular system, central nervous system, deepbrain Adrenergic Receptor Orgasm, Libido Yohimbine Digestive system,Antagonist vascular system, central nervous system, deep brain

TABLE 8 Erectile Dysfunction Action Drug Class Specific Drug DeliverySite Smooth Muscle Enzyme Inhibitor Sildenafil, Digestive RelaxantVardenafil, system, vascular Tadalafil, system, penis Yohimbine VascularDilator, Vascular Dilator, Prostagladin, Digestive system, Smooth MuscleSmooth Muscle Phentolamine vascular system, Relaxant Relaxant penisLibido, Sexual Hormone Estrogen, Digestive system, Arousal Replacementtestosterone vascular system, penis

TABLE 9 Premature Ejaculation Action Drug Class Specific Drug DeliverySite Delayed Selective Sertraline, Digestive system, EjaculationSerotonin Paroxetine vascular system, Reuptake central nervous Inhibitorsystem, penis Delayed Tricyclic Clomipramine Digestive system,Ejaculation Antidepressants vascular system, central nervous system,penis

TABLE 10 Prostatitis Action Drug Class Specific Drug Delivery SiteBacterial Antibiotic Flouroquinolones, Digestive system, EliminationTrimethoprimsulfamet vascular system, hoxazole prostate Pain reliefAnalgesic Aspirin, Central nervous acetaminophen, system, pudendalphenazopyridine, nerves, sacral nerves opioid medications such asmeperidine, hydromorphone, methandone, levorphanol, morphine

FIGS. 11A through 11G show various embodiments of first and secondelectrical stimulation pulse regimes and first and second drug deliveryregimes of the present invention. FIG. 11A illustrates an electricalstimulation pulse regime being applied to a first electrical stimulationsite and a drug bolus being delivered to a first target tissue volume.One example where such an electrical pulse regime and drug deliveryregime could be employed is periodic electrical stimulation to treatincontinence and the delivery of a patient-activated drug bolus for painrelief.

FIG. 11B shows periodic electrical stimulation applied to a firstelectrical stimulation site and periodic drug delivery to a first targettissue volume. One example where such an electrical pulse regime anddrug delivery regime could be employed is periodic electricalstimulation to treat incontinence and periodic drug delivery to treatinterstitial cystitis.

FIG. 11C shows periodic electrical stimulation applied to a firstelectrical stimulation site, periodic drug delivery to a first targettissue volume, and bolus drug delivery to a second target tissue volume.One example where such an electrical pulse regime and drug deliveryregime could be employed is electrical stimulation for the treatment ofincontinence, drug delivery for the treatment of pain, and the deliveryof a patient-activated drug bolus to treat sexual dysfunction.

FIG. 11D shows periodic drug delivery to a first target tissue volume.One example where such a drug delivery regime could be employed is thedelivery of one or more drugs to a target tissue volume for thetreatment of prostatitis.

FIG. 11E shows continuous drug delivery to a target tissue volume. Oneexample where such a drug delivery regime could be employed is thedelivery of one or more drugs to the bladder for the treatment ofinterstitial cystitis.

FIG. 11F shows periodic drug delivery to a first target tissue volumeand continuous drug delivery to a second tissue volume. One examplewhere such a drug delivery regime could be employed is the periodicdelivery of a first drug for the treatment of pelvic pain and thecontinuous delivery of a second drug for the treatment of interstitialcystitis.

FIG. 11G shows periodic electrical stimulation being applied to a firstelectrical stimulation site, periodic electrical stimulation beingapplied to a second electrical stimulation site, and the delivery of abolus of one or more drugs to a first target tissue volume. One examplewhere such an electrical stimulation and drug delivery regime could beemployed is periodic electrical stimulation at a first stimulation sitefor the treatment of fecal incontinence, periodic electrical stimulationat a second electrical stimulation site for the treatment of urinaryincontinence, and the delivery of a patient-activated bolus of one ormore drugs for the treatment of erectile dysfunction.

The various embodiments of the present invention described and shownthus far may be adapted and modified to permit the use of a number ofdifferent communication schemes. Accordingly, incorporated by referenceherein, in its entirety, is U.S. Patent No. patent application No.20020082665A1 to Haller et al. published Jun. 27, 2002 entitled “Systemand Method of Communicating between an Implantable Medical Device and aRemote Computer System or Health Care Provider,” which patentapplication teaches methods and devices that may be adapted for use insome embodiments of the present invention. In the present invention itis contemplated that the methods and devices described hereinabove beextended to include the various communication systems of Haller et al.for, by way of example, one or more of monitoring the performance of INS10 and/or an implantable drug pump implanted within the body of apatient, monitoring the health of the patient and remotely delivering anelectrical stimulation and/or drug therapy to the patient through INS 10and/or implantable or external drug pump 310, INS 10 and/or implantableor external drug pump 310 being capable of bi-directional communicationwith a communication module located external to the patient's body, thesystem comprising: (a) INS 10 and/or implantable or external drug pump310; (b) a communication module; (c) a mobile telephone or similardevice operably connected to the communication module and capable ofreceiving information therefrom or relaying information thereto; (e) aremote computer system, and (f) a communication system capable ofbi-directional communication.

The preceding specific embodiments are illustrative of the practice ofthe invention. It is to be understood, therefore, that other expedientsknown to those skilled in the art or disclosed herein may be employedwithout departing from the invention or the scope of the appendedclaims.

In the claims, means plus function clauses are intended to cover thestructures described herein as performing the recited function and theirequivalents. Means plus function clauses in the claims are not intendedto be limited to structural equivalents only, but are also intended toinclude structures which function equivalently in the environment of theclaimed combination. All printed publications and patents referencedhereinabove are hereby incorporated by referenced herein, each in itsrespective entirety.

1. A method of treating at least one diagnosed pelvic floor disorder ina patient, the at least one disorder being selected from the groupconsisting of constipation, prostatitis, prostatalgia and prostatodynia,the method comprising: implanting a distal end of a first implantablemedical electrical lead in a first tissue volume of the patientadjacent, around or in one of a right pudendal nerve or branches orportions thereof, a left pudendal nerve or branches or portions thereof,a right sacral nerve or branches or portions thereof, or a left sacralnerve or branches or portions thereof, wherein the first lead comprisesat least a first electrode; operably connecting a proximal end of thefirst lead to an hermetically sealed implantable electrical pulsegenerator configured to provide at least a first electrical stimulationpulse regime via at least the first lead; implanting the implantablepulse generator within the patient; implanting a distal end of animplantable drug catheter in one of the first tissue volume or a secondtissue volume of the patient adjacent, around or in one of the rightpudendal nerve or branches or portions thereof, the left pudendal nerveor branches or portions thereof, the right sacral nerve or branches orportions thereof, or the left sacral nerve or branches or portionsthereof; implanting an hermetically sealed implantable drug pump withinthe patient, the implantable drug pump configured to receive and house avolume of a drug therewithin, and to deliver a such drug to an exteriorthereof via the implantable drug catheter; operably connecting aproximal end of the implantable drug catheter to the implantable drugpump; delivering, from the implantable pulse generator, first electricalstimulation pulses to one of the right pudendal nerve or branches orportions thereof, the left pudendal nerve or branches or portionsthereof, the right sacral nerve or branches or portions thereof, or theleft sacral nerve or branches or portions thereof through the first leadand at least the first electrode, the first pulses being provided inaccordance with the first electrical stimulation pulse regime; anddelivering from the implantable drug pump a predetermined portion of thedrug housed therewithin to the exterior thereof through the implantabledrug catheter and to the distal end thereof to one of the right pudendalnerve or branches or portions thereof, the left pudendal nerve orbranches or portions thereof, the right sacral nerve or branches orportions thereof, or the left sacral nerve or branches or portionsthereof; wherein the combination of the first electrical pulse regimeand the predetermined amount of the drug is delivered in a configurationeffective to provide at least partial relief from at least one ofconstipation, prostatitis, prostatalgia and prostatodynia.
 2. The methodof claim 1, wherein the first lead comprises a beam steering leadcomprising multiple electrodes.
 3. The method of claim 1, wherein theimplantable pulse generator and the first lead are capable of generatingand delivering electrical pulses having frequencies ranging betweenabout 50 Hz and about 100 Hz, between about 10 Hz and about 250 Hz, orbetween about 0.5 Hz and about 500 Hz.
 4. The method of claim 1, whereinthe implantable pulse generator and the first lead are capable ofgenerating and delivering electrical pulses having amplitudes rangingbetween about 1 Volt and about 10 Volts, between about 0.5 Volts andabout 20 Volts, or between about 0.1 Volts and about 50 Volts.
 5. Themethod of claim 1, wherein the implantable pulse generator and at thefirst lead are capable of generating and delivering electrical pulseshaving pulse widths ranging between about 180 microseconds and about 450microseconds, between about 100 microseconds and about 1000microseconds, or between about 10 microseconds and about 5000microseconds.
 6. The method of claim 1, wherein delivering firstelectrical stimulation pulses comprises: generating a plurality ofdifferent electrical signals, electrical pulses of the electricalsignals having respective spatial or temporal phases; and delivering thepulses to one of the right pudendal nerve or branch or portions thereof,the left pudendal nerve or branches or portions thereof, the rightsacral nerve or branches or portions thereof, or the left sacral nerveor branches or portions thereof.
 7. The method of claim 1, wherein atleast one of activation, modification and termination of the first pulseregime is carried out by the patient or a health care giver.
 8. Themethod of claim 7, wherein the at least one of activation, modificationand termination of the first pulse regime is carried out in response topatient symptoms appearing or disappearing, or the patient feeling ornot feeling symptoms.
 9. The method of claim 7, wherein patient orhealth care giver activation, modification and/or termination of thefirst pulse regime is accomplished though infra-red, telemetric, radio,magnetic, or ultrasonic means.
 10. The method of claim 1, wherein thefirst pulse regime is delivered in response to a sensed physicalparameter or symptom.
 11. The method of claim 1, wherein the first pulseregime is one of activated, modified and terminated in response to aphysical parameter or symptom being sensed.
 12. The method of claim 11,wherein the physical parameter is sensed using a nerve electrical signalsensor.
 13. The method of claim 1, wherein the drug pump is aperistaltic drug pump.
 14. The method of claim 1, wherein theimplantable drug pump and the implantable pulse generator are disposedwithin a single hermetically sealed housing.
 15. The method of claim 1,wherein the portion of the drug is delivered to one of the rightpudendal nerve or branches or portions thereof, the left pudendal nerveor branches or portions thereof, the right sacral nerve or branches orportions thereof, or the left sacral nerve or branches or portionsthereof at a predetermined relatively constant rate.
 16. The method ofclaim 1, wherein the portion of the drug is delivered to one of theright pudendal nerve or branches or portions thereof, the left pudendalnerve or branches or portions thereof, the right sacral nerve orbranches portions thereof, or the left sacral nerve or branches orportions thereof at predetermined intervals.
 17. The method of claim 1,wherein the drug catheter is structurally combined with the first lead.18. The method of claim 1, wherein the drug is selected from the groupconsisting of anticholinergic drugs, antidepressant drugs, motor neuronsuppression drugs, sensory desensitization drugs, anti-inflammatorydrugs, pain relief drugs and hormone drugs.
 19. The method of claim 1,wherein the drug is selected from the group consisting of tolterodine,hyoscyamine, imipramine, baclofen, resiniferatoxin, dimethyl sulfoxide,bacillus Calmette-Guerin (BCG) and estrogen.
 20. The method of claim 1,wherein the drug is selected from the group consisting of and estrogen.21. The method of claim 1, wherein the drug is selected from the groupconsisting of an antibiotic, an analgesic, a tricyclic antidepressant, amuscle relaxant, a smooth muscle relaxant, and a hormone replacement.22. The method of claim 1, wherein the drug is selected from the groupconsisting of flouroquinolone, trimethoprimsulfamethoxazole, aspirin,acetaminophen, phenazopyridine, opioids, meperidine, hydromorphone,methandone, levorphanol and morphine.
 23. The method of claim 1, whereinthe drug is selected from the group consisting of glucosamine,chondroitin, quercetin, a combination of chondroitin and quercetin,hyaluronic acid, pentosan polysulfate sodium, heparin sodium,amitriptyline, deipramine, nortriptyline, doxepin, impramine,hyoscyamine, oxybutynin chloride, cyclobenzprine, hyoscyamine sulfate,tolterodine tartrate and resiniferatoxin.
 24. The method of claim 1,wherein the drug comprises a motility stimulation agent.
 25. The methodof claim 1, wherein the drug is selected from the group consisting oftagaserod, cisapride, erythomycin, and caffeine.
 26. The method of claim1, further comprising: configuring and providing the hermetically sealedimplantable electrical pulse generator so as to provide a secondelectrical stimulation pulse regime via a second implantable medicalelectrical lead.
 27. The method of claim 26, further comprising:providing the second implantable medical electrical lead, the secondlead comprising proximal and distal ends and at least a secondelectrode.
 28. The method of claim 27, further comprising: implantingthe second lead in the second tissue volume of the patient adjacent,around or in one of the right pudendal nerve or branches or portionsthereof, the left pudendal nerve or branches or portions thereof theright sacral nerve or branches or portions thereof, or the left sacralnerve or branches or portions thereof; operably connecting the proximalend of the second lead to the implantable pulse generator; anddelivering, from the implantable pulse generator, second electricalstimulation pulses to one of the right pudendal nerve or branches orportions thereof, the left pudendal nerve or branches or portionsthereof, the right sacral nerve or branches or portions thereof, or theleft sacral nerve or branches or portions thereof through the secondlead and at least the second electrode, the second pulses being providedin accordance with the second electrical stimulation pulse regime;wherein the combination of the first and the second electrical pulseregimes delivered, and the predetermined amount of the drug is deliveredin a configuration effective to provide at least partial relief from atleast one of constipation, prostatitis, prostatalgia and prostatodynia.29. The method of claim 28, wherein delivering first electricalstimulation pulses comprises delivering the first electrical stimulationpulses to the pudendal nerves the sacral nerves, and delivering secondelectrical stimulation pulses comprises delivering the second electricalstimulation pulses to the other of the pudendal nerves or the sacralnerves.
 30. The method of claim 28, wherein the first and second tissuevolumes are located in respective ones of right and left sides of thepatient.
 31. The method of claim 1, wherein delivering first electricalstimulation pulses comprises delivering the first electrical stimulationpulses to the pudendal nerves or branches or portions thereof.
 32. Themethod of claim 1, wherein delivering first electrical stimulationpulses comprises delivering the first electrical stimulation pulses tothe sacral nerves or branches or portions thereof.
 33. The method ofclaim 1, wherein implanting the implantable drug catheter comprisesimplanting the catheter in the second tissue volume, wherein deliveringfirst electrical stimulation pulses comprises delivering the firstelectrical stimulation pulses to one of the pudendal nerves or one ofthe sacral nerves, and delivering a predetermined portion of the drugcomprises delivering the predetermined portion of the drug to the otherof the pudendal nerves or the sacral nerves.
 34. The method of claim 1,wherein implanting the implantable drug catheter comprises implantingthe catheter in the second tissue volume, wherein the first and secondtissue volumes are located in respective ones of right and left sides ofthe patient.
 35. The method of claim 1, wherein delivering, from theimplantable pulse generator, first electrical stimulation pulsescomprises delivering stimulation pulses at a frequency greater thanapproximately 50 Hz.
 36. A method of treating at least one diagnosedpelvic floor disorder in a patient, the at least one disorder beingselected from the group consisting of constipation, sexual dysfunction,orgasmic dysfunction, erectile dysfunction, prostatitis, prostatalgiaand prostatodynia, the method comprising: implanting a distal end of atleast a first implantable medical electrical lead in a first tissuevolume of the patient adjacent, around or in one of a right pudendalnerve or branches or portions thereof or a left pudendal nerve orbranches or portions thereof, wherein the first lead comprises at leasta first electrode; operably connecting a proximal end of the first leadto an hermetically sealed implantable electrical pulse generatorconfigured to provide at least a first electrical stimulation pulseregime via at least the first lead; implanting the implantable pulsegenerator within the patient; implanting a distal end of an implantabledrug catheter in one of the first tissue volume or a second tissuevolume of the patient adjacent, around or in one of the right pudendalnerve or branches or portions thereof or the left pudendal nerve orbranches or portions thereof; implanting an hermetically sealedimplantable drug pump within the patient, the implantable drug pumpconfigured to receive and house a volume of a drug therewithin, and todeliver a such drug to an exterior thereof via the implantable drugcatheter; operably connecting a proximal end of the implantable drugcatheter to the implantable drug pump; delivering, from the implantablepulse generator, first electrical stimulation pulses to one of a rightpudendal nerve or branches or portions thereof or a left pudendal nerveor branches or portions thereof through the first lead and at least thefirst electrode, the first pulses being provided in accordance with thefirst electrical stimulation pulse regime; delivering from theimplantable drug pump a predetermined portion of the drug housedtherewithin to the exterior thereof through the implantable drugcatheter and to the distal end thereof to one of a right pudendal nerveor branches or portions thereof or a left pudendal nerve or branches orportions thereof; wherein the combination of the first electrical pulseregime and the predetermined amount of the drug is delivered in aconfiguration effective to provide at least partial relief from at leastone of constipation, sexual dysfunction, orgasmic dysfunction, erectiledysfunction, prostatitis, prostatalgia and prostatodynia.
 37. The methodof claim 36, wherein implanting the implantable drug catheter comprisesimplanting the catheter in the second tissue volume, wherein deliveringfirst electrical stimulation pulses comprises delivering the firstelectrical stimulation pulses to the right pudendal nerve or the leftpudendal nerve, and delivering a predetermined portion of the drugcomprises delivering the predetermined portion of the drug to the otherof the right pudendal nerve or the left pudendal nerve.
 38. The methodof claim 36, further comprising delivering second electrical stimulationpulses from the implantable pulse generator to at least portions of thesecond tissue volume via a second implantable medical lead implanted inthe second tissue volume.
 39. The method of claim 38, wherein deliveringfirst electrical stimulation pulses comprises delivering the firstelectrical stimulation pulses to the right pudendal nerve or the leftpudendal nerve, and delivering second electrical stimulation pulsescomprises delivering the second electrical stimulation pulses to theother of the right pudendal nerve or the left pudendal nerve.
 40. Amethod of treating at least one diagnosed pelvic floor disorder in apatient, the at least one disorder being selected from the groupconsisting of prostatalgia and prostatodynia, the method comprising:implanting a distal end of a first implantable medical electrical leadin a first tissue volume of the patient adjacent, around or in one of aright pudendal nerve or branches or portions thereof, a left pudendalnerve or branches or portions thereof, a right sacral nerve or branchesor portions thereof, or a left sacral nerve or branches or portionsthereof, wherein the first lead comprises at least a first electrode;operably connecting a proximal end of the first lead to an hermeticallysealed implantable electrical pulse generator configured to provide atleast a first electrical stimulation pulse regime via the first lead;implanting the implantable pulse generator within the patient;implanting a distal end of an implantable drug catheter in one of thefirst tissue volume or a second tissue volume of the patient adjacent,around or in one of the right pudendal nerve or branches or portionsthereof, the left pudendal nerve or branches or portions thereof, theright sacral nerve or branches or portions thereof, or the left sacralnerve or branches or portions thereof; implanting an hermetically sealedimplantable drug pump within the patient, the implantable drug pumpconfigured to receive and house a volume of a drug therewithin, and todeliver such drug to an exterior thereof via the implantable drugcatheter; operably connecting a proximal end of the implantable drugcatheter to the implantable drug pump; delivering, from the implantablepulse generator, first electrical stimulation pulses to one of the rightpudendal nerve or branches or portions thereof, the left pudendal nerveor branches or portions thereof, the right sacral nerve or branches orportions thereof, or the left sacral nerve or branches or portionsthereof through the first lead and at least the first electrode, thefirst pulses being provided in accordance with the first electricalstimulation pulse regime; and delivering from the implantable drug pumpa predetermined portion of the drug housed therewithin to the exteriorthereof through the implantable drug catheter and to the distal endthereof to one of the right pudendal nerve or branches or portionsthereof, the left pudendal nerve or branches or portions thereof, theright sacral nerve or branches or portions thereof, or the left sacralnerve or branches or portions thereof, wherein the combination of thefirst electrical pulse regime and the predetermined amount of the drugis delivered in a configuration effective to provide at least partialrelief from at least one of prostatalgia and prostatodynia.
 41. Themethod of claim 40, wherein implanting the implantable drug cathetercomprises implanting the catheter in the second tissue volume, whereindelivering first electrical stimulation pulses comprises delivering thefirst electrical stimulation pulses to one of the pudendal nerves or thesacral nerves, and delivering a predetermined portion of the drugcomprises delivering the predetermined portion of the drug to the otherof the pudendal nerves or the sacral nerves.
 42. The method of claim 40,wherein implanting the implantable drug catheter comprises implantingthe catheter in the second tissue volume, wherein the first and secondtissue volumes are located in respective ones of right and left sides ofthe patient.